Results 81 to 90 of about 10,650 (163)

Genètica i caos elèctric : el canal de sodi en la Síndrome de Brugada [PDF]

open access: yes, 2008
Títol obtingut de la portada digitalitzadaaConsultable des del TDXIn this work we have investigated the Brugada syndrome caused by mutations in the sodium channel. We have performed clinical and genetic investigations to identify the genetic carriers. We
Brugada, Ramon
core   +1 more source

Phenotypic Expansion of GYG1 ‐Related Disease Presenting as Hypertrophic Cardiomyopathy With Brugada Phenocopy

open access: yes
Glycogen storage disease Type XV (GSD‐XV; OMIM #613507) is an ultra‐rare autosomal recessive disorder caused by biallelic pathogenic variants in GYG1 , typically presenting with late‐onset skeletal myopathy, while ...
Umran Cetincelik   +3 more
core   +1 more source

Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A

open access: yes, 2020
A 30-year-old man presented with intellectual disability associated with epilepsy. The epilepsy was initially treated with sodium valproate and since he was 28 years-old with lamotrigine.
Oliva, A   +19 more
core   +1 more source

Brugada syndrome and p.E61X_RANGRF

open access: yes, 2014
Background: Brugada syndrome is an inherited cardiac condition transmitted with an autosomal dominant pattern which can lead to sudden cardiac death from malignant ventricular arrhythmias.
Iglesias, Anna   +6 more
core   +2 more sources

Fragmentation in Body Surface Potential Mapping Recordings from Patients with Brugada Syndrome [PDF]

open access: yes, 2020
Brugada syndrome ...
MS Guillem   +7 more
core  

Proposed diagnostic criteria for the Brugada syndrome - Consensus report

open access: yes, 2002
Asyndrome characterized by ST-segment elevation in right precordial leads (V1 to V3) that is unrelated to ischemia, electrolyte disturbances, or obvious structural heart disease was reported as early as 1953,1 but was first described as a distinct ...
BRUGADA J   +11 more
core   +1 more source

Brugada syndrome: 1992–2002 A historical perspective

open access: yes, 2003
An intriguing new clinical entity characterized by ST-segment elevation in the right precordial electrocardiographic leads and a high incidence of sudden death in individuals with structurally normal hearts was described by Pedro and Josep Brugada in ...
Pedro Brugada   +11 more
core   +1 more source

Clinical phenotypes in acute and chronic infarction explained through human ventricular electromechanical modelling and simulations

open access: yeseLife
Sudden death after myocardial infarction (MI) is associated with electrophysiological heterogeneities and ionic current remodelling. Low ejection fraction (EF) is used in risk stratification, but its mechanistic links with pro-arrhythmic heterogeneities ...
Xin Zhou   +8 more
doaj   +1 more source

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